Suppr超能文献

日本一线酪氨酸激酶抑制剂耐药和/或不耐受的慢性期慢性髓性白血病的治疗结果:新 TARGET 研究二线结果。

Treatment outcomes of chronic-phase chronic myeloid leukemia with resistance and/or intolerance to a 1st-line tyrosine kinase inhibitor in Japan: the results of the New TARGET study 2nd-line.

机构信息

Division of Hematology, Department of Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582, Japan.

Department of Hematology and Rheumatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.

出版信息

Int J Hematol. 2020 Jun;111(6):812-825. doi: 10.1007/s12185-020-02843-8. Epub 2020 Mar 9.

Abstract

We herein report the results of the New TARGET study 2nd-line, which collected data on patients with chronic-phase (CP) chronic myeloid leukemia (CML) who received a 2nd-line tyrosine kinase inhibitor (TKI) because of resistance and/or to a 1st-line TKI. A total of 98 patients were enrolled intolerance between April 2010 and March 2013, and 82 patients were analyzed. The median age was 54 years (range 22-88 years). Seventy-six patients (93%) received imatinib as the 1st-line TKI. Forty-five (55%) and 37 (45%) patients began nilotinib and dasatinib treatments at entry, respectively. First-line TKI treatment achieved complete hematological response in 79 patients (96%) and complete cytogenetic response (CCyR) in 49 patients (60%), respectively. Nine patients (11%) had BCR-ABL1 kinase domain point mutations at enrollment. The estimated 3-year progression-free-survival rate after enrollment was 98.7% (95% CI 91.1-99.8%). Overall, the probabilities of achieving CCyR and a major molecular response were 89.3% (95% CI 81.4-94.8%) and 87.2% (95% CI 78.1-93.8%), respectively. There were no new safety issues. This study demonstrated that CML-CP patients in Japan who are resistant and/or intolerant to a 1st-line TKI can achieve an extremely good outcome by 2nd-line TKI treatment.

摘要

我们在此报告新 TARGET 研究二线治疗的结果,该研究收集了因耐药和/或不耐受一线 TKI 而接受二线酪氨酸激酶抑制剂(TKI)治疗的慢性期(CP)慢性髓性白血病(CML)患者的数据。共有 98 名患者因不耐受于 2010 年 4 月至 2013 年 3 月入组,其中 82 名患者进行了分析。中位年龄为 54 岁(范围 22-88 岁)。76 名患者(93%)接受伊马替尼作为一线 TKI。45 名(55%)和 37 名(45%)患者分别在入组时开始接受尼洛替尼和达沙替尼治疗。一线 TKI 治疗分别使 79 名患者(96%)实现完全血液学反应和 49 名患者(60%)实现完全细胞遗传学反应(CCyR)。9 名患者(11%)在入组时存在 BCR-ABL1 激酶结构域点突变。入组后 3 年无进展生存率估计为 98.7%(95%CI 91.1-99.8%)。总体而言,实现 CCyR 和主要分子学反应的概率分别为 89.3%(95%CI 81.4-94.8%)和 87.2%(95%CI 78.1-93.8%)。没有新的安全性问题。本研究表明,日本对一线 TKI 耐药和/或不耐受的 CML-CP 患者通过二线 TKI 治疗可获得极好的疗效。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验